Luteoforol

Luteoforol
	Chemical structure of luteoforol
Names
	IUPAC name (2S)-2-(3,4-dihydroxyphenyl)-3,4-dihydro-2H-chromene-4,5,7-triol
	Other names 3-Deoxyleucocyanidin
Identifiers
CAS Number	24897-98-1 ;
3D model (JSmol)	Interactive image ;
ChEBI	CHEBI:27686 ;
ChemSpider	102562 ;
KEGG	C05907 ;
PubChem CID	440834 ;
UNII	830GM1N73B ;
CompTox Dashboard (EPA)	DTXSID901336190 ;
	InChI InChI=1S/C15H14O6/c16-8-4-11(19)15-12(20)6-13(21-14(15)5-8)7-1-2-9(17)10(18)3-7/h1-5,12-13,16-20H,6H2/t12?,13-/m0/s1 Key: FSYDWKPCKNCRDI-ABLWVSNPSA-N;
	SMILES C1C(C2=C(C=C(C=C2OC1C3=CC(=C(C=C3)O)O)O)O)O;
Properties
Chemical formula	C15H14O6
Molar mass	290.26 g/mol
	Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). verify (what is ?) Infobox references

Last updated May 29, 2025

Luteoforol is a chemical compound belonging to the flavan-4-ol class of flavonoids.

Luteoforol is induced in pome fruits by prohexadione-calcium.^[1]

References

↑ Spinelli, Francesco; Speakman, John-Bryan; Rademacher, Wilhelm; Halbwirth, Heidi; Stich, Karl; Costa, Guglielmo (2005). "Luteoforol, a flavan 4-ol, is induced in pome fruits by prohexadione-calciumand shows phytoalexin-like properties against Erwinia amylovora and other plant pathogens" . European Journal of Plant Pathology. 112 (2): 133–142. doi:10.1007/s10658-005-2192-x. S2CID 897040.

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[1] Spinelli, Francesco; Speakman, John-Bryan; Rademacher, Wilhelm; Halbwirth, Heidi; Stich, Karl; Costa, Guglielmo (2005). "Luteoforol, a flavan 4-ol, is induced in pome fruits by prohexadione-calciumand shows phytoalexin-like properties against Erwinia amylovora and other plant pathogens" . European Journal of Plant Pathology. 112 (2): 133–142. doi:10.1007/s10658-005-2192-x. S2CID 897040.

[1]

v t e Types of flavan-4-ols
Flavan-4-ols:	Apiforol Luteoforol
Glycosides	abacopterins A B C D Triphyllin A 6,8-dimethyl-7-hydroxy-4'-methoxyanthocyanidin-5-O-β-d-glucopyranoside

Names
Chemical structure of luteoforol
IUPAC name (2S)-2-(3,4-dihydroxyphenyl)-3,4-dihydro-2H-chromene-4,5,7-triol
Other names 3-Deoxyleucocyanidin
Identifiers
CAS Number	24897-98-1 ^Y
3D model (JSmol)	Interactive image
ChEBI	CHEBI:27686 ^N
ChemSpider	102562
KEGG	C05907
PubChem CID	440834
UNII	830GM1N73B ^Y
CompTox Dashboard (EPA)	DTXSID901336190
InChI InChI=1S/C15H14O6/c16-8-4-11(19)15-12(20)6-13(21-14(15)5-8)7-1-2-9(17)10(18)3-7/h1-5,12-13,16-20H,6H2/t12?,13-/m0/s1 Key: FSYDWKPCKNCRDI-ABLWVSNPSA-N
SMILES C1C(C2=C(C=C(C=C2OC1C3=CC(=C(C=C3)O)O)O)O)O
Properties
Chemical formula	C₁₅H₁₄O₆
Molar mass	290.26 g/mol
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). N verify (what is ^YN ?) Infobox references